Canonical Allele Identifier: CA2206693111

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9764205_9764213delinsAGGGGAGCT , CM000678.2:g.9764205_9764213delinsAGGGGAGCT	GRCh38
NC_000016.9:g.9858062_9858070delinsAGGGGAGCT , CM000678.1:g.9858062_9858070delinsAGGGGAGCT	GRCh37
NC_000016.8:g.9765563_9765571delinsAGGGGAGCT	NCBI36
NG_011812.1:g.423542_423550delinsAGCTCCCCT
NG_011812.2:g.423542_423550delinsAGCTCCCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.3331_3339delinsAGCTCCCCT MANE Select	ENSP00000332549.3:p.Ser1111=
ENST00000535259.6:c.2860_2868delinsAGCTCCCCT	ENSP00000441572.3:p.Ser954=
ENST00000636273.2:n.2924_2932delinsAGCTCCCCT
ENST00000674742.1:c.2860_2868delinsAGCTCCCCT	ENSP00000502200.1:p.Ser954=
ENST00000675398.1:c.*701_*709delinsAGCTCCCCT	ENSP00000502752.1:n.*701_*709delinsAGCTCCCCT
ENST00000330684.3:c.3331_3339delinsAGCTCCCCT	ENSP00000332549.3:p.Ser1111=
ENST00000396573.6:c.3331_3339delinsAGCTCCCCT	ENSP00000379818.2:p.Ser1111=
ENST00000396575.6:c.2920_2928delinsAGCTCCCCT	ENSP00000379820.3:p.Ser974=
ENST00000461292.3:n.2970_2978delinsAGCTCCCCT
ENST00000535259.5:c.2920_2928delinsAGCTCCCCT	ENSP00000441572.2:p.Ser974=
ENST00000562109.5:c.3331_3339delinsAGCTCCCCT	ENSP00000454998.1:p.Ser1111=
NM_000833.4:c.3331_3339delinsAGCTCCCCT	NP_000824.1:p.Ser1111=
NM_001134407.2:c.3331_3339delinsAGCTCCCCT	NP_001127879.1:p.Ser1111=
NM_001134408.2:c.3331_3339delinsAGCTCCCCT	NP_001127880.1:p.Ser1111=
XM_011522456.1:c.3172_3180delinsAGCTCCCCT	XP_011520758.1:p.Ser1058=
XM_011522457.1:c.3073_3081delinsAGCTCCCCT	XP_011520759.1:p.Ser1025=
XM_011522458.1:c.2860_2868delinsAGCTCCCCT	XP_011520760.1:p.Ser954=
XM_011522459.1:c.2860_2868delinsAGCTCCCCT	XP_011520761.1:p.Ser954=
XM_011522460.1:c.2860_2868delinsAGCTCCCCT	XP_011520762.1:p.Ser954=
XM_011522461.1:c.3331_3339delinsAGCTCCCCT	XP_011520763.1:p.Ser1111=
XM_011522458.3:c.2860_2868delinsAGCTCCCCT	XP_011520760.1:p.Ser954=
XM_011522461.3:c.3331_3339delinsAGCTCCCCT	XP_011520763.1:p.Ser1111=
XM_017023172.1:c.3487_3495delinsAGCTCCCCT	XP_016878661.1:p.Ser1163=
XM_017023173.1:c.3487_3495delinsAGCTCCCCT	XP_016878662.1:p.Ser1163=
NM_001134407.3:c.3331_3339delinsAGCTCCCCT MANE Select	NP_001127879.1:p.Ser1111=
NM_000833.5:c.3331_3339delinsAGCTCCCCT	NP_000824.1:p.Ser1111=